Medtronic Inc Medtronic DLP VAD Venous Cannula for Ventricular Assist, Models 95036 and CB95036. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic DLP VAD Venous Cannula for Ventricular Assist, Models 95036 and CB95036.
Brand
Medtronic Inc
Lot Codes / Batch Numbers
Lot numbers 2003080199, 2003090147, 2003100101, 2004010371, and 2004030070.
Products Sold
Lot numbers 2003080199, 2003090147, 2003100101, 2004010371, and 2004030070.
Medtronic Inc is recalling Medtronic DLP VAD Venous Cannula for Ventricular Assist, Models 95036 and CB95036. due to Spiral tip from DLP VAD cannula may be loose and potentially detach during use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Spiral tip from DLP VAD cannula may be loose and potentially detach during use.
Recommended Action
Per FDA guidance
A notification letter dated September 23, 2004 was sent by certified mail to US customers. The letter cautions the customer about the possibility of tip detachment and requests the impacted product to be returned to Medtronic for replacement. Customers are requested to complete a Field Corrective Action Certificate acknowledging the receipt of this information.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026